A General and Stereospecific Synthesis of Trans Alkenes and Regiospecific Synthesis of Ketones via Stepwise Hydroboration

dc.contributor.author Brown, Herbert C.
dc.contributor.author Basavaiah, D.
dc.contributor.author Kulkarni, Surendra U.
dc.date.accessioned 2022-03-27T09:06:15Z
dc.date.available 2022-03-27T09:06:15Z
dc.date.issued 1982-01-01
dc.description.abstract The hydroboration of 1-bromo-1-alkynes with alkylbromoboranes (RBHBr·SMe2), conveniently obtained via the controlled hydridation of alkyldibromoboranes (RBBr2·SMe2), followed by treatment with sodium methoxide produces B-(trans-1-alkyl-1-alkenyl)boronate esters that provide the corresponding trans alkenes on protonolysis and ketones on oxidation. © 1982, American Chemical Society. All rights reserved.
dc.identifier.citation Journal of Organic Chemistry. v.47(19)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo00140a056
dc.identifier.uri https://pubs.acs.org/doi/abs/10.1021/jo00140a056
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12420
dc.title A General and Stereospecific Synthesis of Trans Alkenes and Regiospecific Synthesis of Ketones via Stepwise Hydroboration
dc.type Journal. Letter
dspace.entity.type
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